جستجوی مقالات مرتبط با کلیدواژه « aplasia » در نشریات گروه « پزشکی »

Absent right renal vein is very uncommon. This study aimed to describe a case of the absent right renal vein with drainage from the upper pole of the kidney into the right suprarenal vein and then into the ipsilateral gonadal vein.

A 25-year-old female patient with abdominal pain was referred to the radiology clinic for abdominopelvic computed tomography (CT) with oral and intravenous contrast. On CT images, the right renal vein was absent. The drainage of the right kidney was through the upper pole to the suprarenal vein and thereafter to the right gonadal vein and the inferior vena cava (IVC). Some suprarenal veins were drained to the superior mesenteric vein via collaterals. The IVC diameter, especially the intrahepatic portion, was decreased.

The absence of the right renal vein is very rare, and to the best of our knowledge, drainage from the upper pole into the ipsilateral gonadal vein has not been previously reported in the literature.

Agenesis and hypoplasia of the paranasal sinuses is an anatomical variation that often occurs in frontal sinuses but this rarely happens combined with other paranasal sinuses. The present study was conducted to report a rare case of hypoplasia of the paranasal sinuses and atrophy of all three turbinates in Iran.

CASE REPORT:

 In this study, we report the case of a 28-year-old man who referred with trauma to the head and anosmia. The patient had no complaints of nasal obstruction or congestion, cerebrospinal fluid leakage before or after trauma. He also had no previous history of rhinosinusitis or olfactory disorder. CT scans of nose and paranasal sinuses showed some findings such as bilateral middle and inferior concha atrophy, bilateral hypoplasia of maxillary, ethmoid, sphenoid, and right frontal sinuses and left frontal sinus aplasia. To the best of our knowledge, the number of reports about the combination of abnormal variations of paranasal sinuses was less than 5 and in the present case report, all sinuses had hypoplasia and at the same time, there was turbinate atrophy, while the patient had no clinical symptoms.

According to the present study, pneumatization of sinus is not necessarily associated with clinical symptoms and other factors play a role in sinus function.

Aplasia cutis congenita (ACC) is a rare congenital disorder characterized by localized or widespread skin absence. The most common site is the scalp and the main cause is unknown. Here we report a case of extensive ACC with scalp involvement. A female infant with an Apgar score of 9 and weighing 3406 gr was born by cesarean section in Besat Hospital, Sanandaj, Iran. A lesion measuring 5×10 cm with highly prominent vessels was on the forehead and parietal bone without scalp, skull, or bone tissue leading to the brain tissue being covered with a thin membrane. Other clinical examinations were normal. The newborn suffered from a ruptured aneurysm and intracerebral hemorrhage and underwent pharmacologic treatment. She died after 21 days of hospitalization. In order to prevent mortality in infants with skin defects, infection control is a priority. Antibiotics could be administered in cases with extensive lesions to prevent neonatal sepsis and improve scar tissue formation. Moreover, restorative measures should be taken if necessary.